نتایج جستجو برای: ichthyosis

تعداد نتایج: 1959  

2013
Marcela Sena Teixeira Mendes Samara Silva Kouzak Thaissa Araújo Aquino Gustavo Henrique Soares Takano Antonio de Padua Lima

Epidermolytic ichthyosis is a rare autosomal dominant disease that manifests at birth with fragile blisters and erosions that evolve into hyperkeratotic lesions associated or not with erythroderma. When the disease is associated with a mutation in cytokeratin 1, it may be related to hyperkeratosis of palms and soles, but this is not usually found when cytokeratin 10 is mutated. The disease can ...

Journal: :Cutis 2006
Alessandra B Alió Lynne M Bird Scott D McClellan Bari B Cunningham

Sjögren-Larsson syndrome (SLS) is an autosomal recessive neurocutaneous disorder most commonly seen in the Scandinavian population and characterized by congenital ichthyosis, mental retardation, and spastic diplegia or quadriplegia. We report a case of SLS in an 11-month-old girl of Lebanese and Mexican-Syrian ancestry who presented with ichthyosis, developmental delay, and spasticity. Results ...

2017
Kayo Tanita Taku Fujimura Yota Sato Takanori Hidaka Sadanori Furudate Yumi Kambayashi Akira Tsukada Akira Hashimoto Setsuya Aiba

Acquired ichthyosis (AI) is a reactive cutaneous manifestation that can be associated with malignant hematological disease, including cutaneous T-cell lymphoma (CTCL). Since it is difficult to distinguish AI from ichthyosiform mycosis fungoides, to select the treatment for CTCL with ichthyosis-like appearance and to evaluate its efficacy is sometimes challenging. In this report, we describe a c...

Journal: :The Journal of Nervous and Mental Disease 1883

Journal: :British Journal of Dermatology 1911

Journal: :Proceedings of the Royal Society of Medicine 1933

Journal: :Indian Journal of Paediatric Dermatology 2018

2009
SJ Brown CL Relton H Liao Y Zhao A Sandilands WHI McLean HJ Cordell NJ Reynolds

BACKGROUND Null mutations within the filaggrin gene (FLG) cause ichthyosis vulgaris and are associated with atopic eczema. However, the dermatological features of filaggrin haploinsufficiency have not been clearly defined. OBJECTIVES This study investigated the genotype-phenotype association between detailed skin phenotype and FLG genotype data in a population-based cohort of children. METH...

Journal: :Orphanet journal of rare diseases 2016
Andrea Diociaiuti May El Hachem Elisa Pisaneschi Simona Giancristoforo Silvia Genovese Pietro Sirleto Renata Boldrini Adriano Angioni

BACKGROUND The term ichthyosis describes a generalized disorder of cornification characterized by scaling and/or hyperkeratosis of different skin regions. Mutations in a broad group of genes related to keratinocyte differentiation and epidermal barrier function have been demonstrated to play a causative role in disease development. Ichthyosis may be classified in syndromic or non-syndromic form...

Journal: :Journal of the College of Physicians and Surgeons--Pakistan : JCPSP 2011
Nasser Rashid Dar Naeem Raza Azmat Khan Muhammad Umar Amin

Black brown hyperpigmentation of the mucosae, sunexposed skin, palmar creases and frictional sites (Addisonian pigmentation) is characteristic of Addison disease. However, it can also occur as a paraneoplastic manifestation of tumours like bronchogenic carcinoma. Acquired ichthyosis starts later in life and can also be a paraneoplastic presentation. We report a unique combination of paraneoplas...

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